Devices, methods and systems for establishing supplemental blood flow in the circulatory system

ABSTRACT

A cannula for insertion through a biologic tissue. The cannula includes a shaft having proximal and distal end portions with a lumen therebetween. The cannula further includes a tip having a proximal end portion, a distal tip end, and a lumen therebetween. The proximal end portion of the tip is secured to the distal end portion of the shaft so that the lumen of the tip is in fluid communication with the lumen of the shaft. The tip includes an opening that extends proximally relative to the distal tip end to permit the flow of fluid into the lumen of the tip even in the event that the distal tip end becomes obstructed.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit of U.S. Provisional PatentApplication Ser. No. 61/303,351, filed on Feb. 11, 2010, the disclosureof which is incorporated by reference herein.

TECHNICAL FIELD

This invention relates generally to medical devices and methods and,more particularly, to devices and methods for assisting conduction ofbodily fluids.

BACKGROUND

Various devices and methods have been utilized to assist in conductingbodily fluids. For instance, blood pumps with inflow and outflowcannulae assist the heart in circulating blood in a patient experiencingcongestive heart failure and a transplant organ has either not beenlocated or the patient is not a suitable candidate for the transplant.Accordingly, the blood pump may be fluidically attached to the left sideof the heart and then located remotely, such as subcutaneously orsubmuscularly in a manner similar to a pacemaker, in what is referred toas a “pump pocket.” The pump pocket may be generally located at aposition that is accessible by a surgical incision from below thecollarbone, over the pectoral muscle, and toward the breast. A cannulamay then be used to fluidically couple the heart to the pump. In stillanother example, a cannula is inserted into the bladder or kidney, suchas in dialysis or urinary obstruction or infection.

Yet, known conventional cannula designs are susceptible to obstructionby adjacent biologic tissue. Therefore, there is a continuing need todevelop cannulae to address these and other challenges associated withconventional cannulae and supplemental fluid flow systems.

SUMMARY

In one illustrative embodiment, the invention is directed to a cannulafor insertion through a biological tissue. The cannula includes a shafthaving proximal and distal end portions with a lumen therebetween. Thecannula further includes a tip having a proximal end portion, a distaltip end, and a lumen therebetween. The proximal end portion of the tipis secured to the distal end portion of the shaft so that the lumen ofthe tip is in fluid communication with the lumen of the shaft. The tipincludes an opening communicating with the lumen and extendingproximally relative to the distal tip end to permit the flow of fluidinto the lumen of the tip even in the event that the distal tip endbecomes obstructed.

The opening that extends proximally may be at least one notch in the tipextending between the lumen and an outer surface of the tip, at leastone aperture that extends between the lumen and the outer surface of thetip, an inclined edge that is angled relative to a lengthwise centralaxis of the tip, or a combination of the same.

In another illustrative embodiment, the invention is directed to a bloodcirculation assist system that includes the cannula, which extends froma pump to the heart of a patient. The assist system further includes anoutflow cannula that extends from the pump to an artery of the patient.

In accordance with another illustrative embodiment, the invention isdirected to a method of communicating fluid into a lumen of a cannulathat includes a distal tip. The method comprises inserting the distaltip through a biologic tissue and into a cavity. Fluid is drawn from thecavity and into the tip through an opening in the distal tip of thecannula. The opening in the distal tip extends proximally relative tothe distal tip end of the distal tip.

Yet another illustrative embodiment of the invention is directed to amethod of preventing fluid flow obstruction in a cannula having a lumenand a distal tip. The method comprises inserting the distal tip througha biologic tissue and into a cavity. Fluid is drawn from the cavity andinto the tip through an opening in the distal tip of the cannula. Theopening in the distal tip extends proximally relative to the distal tipend of the distal tip. The fluid continues to be drawn from the cavityand into the lumen through the opening when the distal tip of thecannula is occluded by an adjacent biologic tissue.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a schematic representation of chest anatomy and illustratesone example of a pathway, exterior to the vascular system, used toaccess a patient's heart and to implant a circulatory assist system thatis coupled to the aortic arch in accordance with an embodiment of theinvention.

FIG. 1B is a schematic representation of another exemplary embodimentthat is similar to FIG. 1A, but with the circulatory assist systemcoupled to the subclavian artery.

FIG. 1C is a schematic representation of yet another exemplaryembodiment that is similar to FIG. 1A, but with the circulatory assistsystem coupled to the descending aorta at a location inferior to theheart and in close proximity to the iliac arteries.

FIG. 2 is a side-elevational view of one exemplary embodiment of aninflow cannula having a cannula tip.

FIG. 3 is an enlarged perspective view of the cannula tip shown in FIG.2.

FIG. 4 is a cross-sectional view through the diameter of the inflowcannula, taken along the line 4-4 in FIG. 2.

FIG. 4A is a cross-sectional view of an inner liner of the inflowcannula, taken along the line 4A-4A in FIG. 4.

FIG. 5 is a side-elevational view of a hub of the inflow cannula shownin FIG. 2.

FIGS. 6A-6D are enlarged cross-sectional views illustrating successivesteps of an exemplary method of surgically implanting a cannula tip intothe left ventricle of the heart.

FIG. 7 is a perspective view of the inflow cannula including anotherembodiment of a cannula tip.

FIG. 8 is a perspective view of the inflow cannula including yet anotherembodiment of a cannula tip.

FIG. 8A is a side-elevational view of the cannula tip shown in FIG. 8,depicting the angle of inclination of a distal end surface of thecannula tip.

FIG. 9 is a perspective view of the inflow cannula including anotherembodiment of a cannula tip for use in a trans-septal procedure.

FIG. 9A is an enlarged cross-sectional view of the cannula tip of FIG. 9implanted across the intra-atrial septum.

FIG. 10 is a perspective view of the inflow cannula including anothertransseptal embodiment of the cannula tip.

FIG. 10A is an enlarged cross-sectional view of the cannula tip of FIG.10 implanted across the intra-atrial septum.

FIG. 11 is a perspective view of the inflow cannula including yetanother transseptal embodiment of the cannula tip.

FIG. 11A is an enlarged cross-sectional view of the cannula tip of FIG.11 implanted across the intra-atrial septum.

DETAILED DESCRIPTION

FIG. 1A illustrates one of many possible general configurations of ablood circulation assist system 10. The devices and systems configuredin accordance with the teachings herein may be implanted in any suitablesurgical manner, including but not limited to those discussed generallyherein, and may be used in association with other biologic tissues, forexample, an interior chamber of a kidney (not shown) or still otherbiological tissues through which a cavity or chamber may be accessed andfluid withdrawn.

The system 10 may be used to pump blood from a chamber containingoxygenated blood of the heart 20 of a patient 22 (i.e., the left side ateither the left atrium 24 or the left ventricle 26) and into thepatient's arterial system, thereby “unloading” the heart 20 that hasbeen weakened due to disease or genetic defect. The system 10 includes ablood pump 28 having an inlet 30 and an outlet 32. The pump 28 may beimplanted in either the left or right side of the patient 22(implantation in the left side is shown) or remain external to thepatient's body. The pump 28 may include a power cord 34 that extendstransdermally from the pump 28 to a position in the abdomen where thepower cord 34 exits the patient 22 and connects to a power source (notshown). Various blood pump designs are known and may be used, includingthe conventional designs described in U.S. Pat. No. 6,176,848 issued toRau et al. on Jan. 23, 2001, and entitled “Intravascular Blood Pump”;U.S. Pat. No. 6,116,862 issued to Rau et al. on Sep. 12, 2000, andentitled “Blood Pump”; U.S. Pat. No. 6,942,611 issued to Siess on Sep.13, 2005, and entitled “Paracardiac Blood Pump”; U.S. Pat. No. 6,623,475issued to Siess on Sep. 23, 2003, and entitled “Blood Pump WithoutBearing”; and German Publ. No. DE102004019721 that was published on Oct.6, 2005, and is entitled “Pump,” the disclosures of which areincorporated herein by reference in their entireties.

The system 10 further includes an outflow cannula 36 that connects theoutlet 32 of the pump 28 to an artery, such as the aorta 38, at anarterial access site 39 a, shown in FIG. 1A as being superior to theheart 20. Alternatively, the outflow cannula 36 may be connected to anarterial access site 39 b that is located in the left subclavian artery40, as shown in FIG. 1B. In the configurations shown in FIGS. 1A and 1B,the pump 28 may be superficially implanted in a pump pocket 42 a. Asanother alternative and as shown in FIG. 10, the outflow cannula 36 maybe connected to an arterial access site 39 c in the descending aorta 44and in close proximity to the left and right iliac arteries 46, 48. Inthis case, the pump 28 may be superficially implanted at a pump pocket42 b located in the abdomen of the patient 22. The outflow cannula 36may be connected to the selected artery through a suitable surgicalprocedure that may involve the use of suitable grafts (not shown) and/orsuturing (not shown).

Referring again to FIG. 1A, an inflow cannula 50 connects the inlet 30of the pump 28 to an exterior wall of the heart 20, such as a wall 52 ofthe left ventricle 26. The inflow cannula 50 may be directed into theheart 20 through any desired surgical approach, such as one of theapproaches subsequently discussed.

The outflow and inflow cannulae 36, 50 may be connected to the outlet 32and inlet 30 of the blood pump 28, respectively, prior to or afterimplantation of the pump 28. In that regard, the cannulae 36, 50 may befirst cut to a suitable length by an appropriate sterilized cutting tool(not shown) such that the system 10 may be more easily implanted withoutkinking of the cannulae 36, 50. The inflow cannula 50 may be configuredto facilitate cutting to the desired length, as subsequently discussed.

In operation, blood may be pumped from the left ventricle 26, throughthe inflow cannula 50 to the pump 28, and from the pump 28 to theselected artery (the aorta 38 in FIG. 1A, the left subclavian artery 40in FIG. 1B, the descending aorta 44 in FIG. 10, or other as desired).

For illustrative and reference purposes, certain additional anatomy isshown, including a right atrium 54 and a right ventricle 56 on the rightside of the heart 20. The right atrium 54 receives blood from the venousnetwork, generally, and more specifically, as shown, the left and rightsubclavian veins 58, 60, the left and right jugular veins 62, 64, andthe superior and inferior vena cavae 66, 68. Blood moves from the rightatrium 54 to the right ventricle 56 and is then pumped to the lungs (notshown) to be oxygenated. Blood returning from the lungs enters the leftatrium 24 of the heart 20 through the pulmonary veins 70. The bloodwithin the left atrium 24 moves into the left ventricle 26 and is pumpedinto the aorta 38 and the arterial system beyond, including the leftsubclavian artery 40, the left common carotid 72, and thebrachiocephalic trunk 74 leading to the right common carotid 76 and theright subclavian artery 78.

Turning now to FIG. 2, and with continued reference to FIG. 1A, theinflow cannula 50 is shown in greater detail. The inflow cannula 50includes a tip 110 that is configured to be inserted through a biologictissue, such as the wall 52 of the left ventricle 26. The tip 110includes a lumen 112 extending between proximal and distal end portions114, 116. The inflow cannula 50 also includes a shaft 120 having a lumen122 extending between proximal and distal end portions 124, 126. Theinflow cannula 50 still further includes a hub 130 having a lumen 132extending between proximal and distal end portions 134, 136. The distalend portion 126 of the shaft 120 is coupled to the proximal end portion114 of the tip 110, and the proximal end portion 124 of the shaft 120 iscoupled to the distal end portion 136 of the hub 130. The hub 130 may bemolded directly to the proximal end portion 124 of the shaft 120 or,alternatively, the hub 130 may be constructed separately and thenaffixed to the proximal end portion 124 with a biocompatible adhesive.The lumens 112, 122, 132 align to be collinear and in fluidiccommunication. The lumens 112, 122, 132 may have the same diameter toeliminate steps or other discontinuities in order to minimize thrombusformation and flow restriction therein.

The proximal end portion 134 of the hub 130 may be configured to becoupled to the inlet 30 of the blood pump 28, as shown in FIG. 1A, andsuch that blood may flow from the left ventricle 26 of the heart 20,through the lumens 112, 122, 132 and to the inlet 30 of the blood pump28. The blood may then be pumped through the outflow cannula 36 to thedesired artery, such as the aorta 38, descending aorta 44, or the leftsubclavian artery 40 as described previously in conjunction with FIGS.1A, 1B, and 1C.

The tip 110 may be constructed from a metallic material, such astitanium, a titanium alloy, stainless steel, or platinum. The tip 110when constructed from a metallic material may include a sintered sectionor at least a portion covered by a fabric that promotes the in-growth oftissue. Alternatively, the tip 110 may be molded from a thermosetmaterial, such as silicone, or a thermoplastic material, such aspolyurethane. An example of a polyurethane that may be used isCARBOTHANE (Lubrizol Advanced Materials, Inc., Cleveland, Ohio). If arelatively conformable design is desired, the tip 110 may be constructedfrom a thermoset or thermoplastic material having a durometer rangingfrom about shore 25 A to about shore 90 A. If a relatively rigid designis desired, the tip 110 may be constructed from a thermoset orthermoplastic material having a durometer ranging from about shore 55 Dto about shore 90 D.

To further minimize the chance of thrombus formation, the moldingprocess may include an insert molding process that eliminates partinglines, i.e., those places where a mismatch of material may occur. Use ofthe insert molding process results in a luminal surface, which is indirect contact with blood flowing through the tip 110, that is smoothand seamless. Accordingly, it is not necessary to coat an inner surfaceof the lumen 112 with an anti-thrombotic material, yet the coatings maybe included if so desired.

To increase hemocompatibility, the distal end portion 116 of the tip 110may be polished to minimize irregularities resulting from the machiningprocess. The highly polished surface minimizes proliferation of tissuegrowth, hence minimizing the likelihood that tissue will grow over thetip 110 and occlude blood flow into the inflow cannula 50.

Referring still to FIG. 2 and now also to FIG. 3 where additionaldetails of the tip 110 may be seen. The distal end portion 116 of thetip 110 is configured to be inserted into a chamber of the patient'sheart 20 (FIG. 1A). In that regard, while the diameter of the lumen 112may be constant throughout the length of both the proximal and distalend portions 114, 116 of the tip 110, an outer surface 138 of the tip110 may be discontinuous. One such discontinuity, a shoulder 140, may bepositioned between the proximal and distal end portions 114, 116 and isconfigured to be positioned against an inside surface of the wall 52(FIG. 1A) of the heart 20 (FIG. 1A) when the distal end portion 116 isinserted into, for example, the left ventricle 26 (FIG. 1A). Thiscontrols the length of the distal end portion 116 inserted in thechamber and ensures that the distal end portion 116 is not dislodgedfrom the chamber prior to suturing of the tip 110 to the wall 52 (FIG.1A) of the heart 20 (FIG. 1A).

The outer surface 138 may converge, or taper, such as a frusto-conicalshape, between the shoulder 140 and the distal end portion 116 to distaltip end 142. The distal tip end 142 may be constructed, or molded, asshown, to be substantially orthogonal to a lengthwise central axis 144of the tip 110. This arrangement permits blood to be continuouslywithdrawn from the left ventricle 26 (FIG. 1A); however, a variety ofalternative structure are possible, including the subsequently discussedalternative tips.

The tip 110 further includes an opening 146 extending proximallyrelative to the distal tip end 142 that is configured to permit blood tobe continuously drawn into the lumen 112 of the tip 110, even when thedistal tip end 142 of the tip 110 becomes obstructed or occluded, suchas by adjacent internal heart tissue. The opening 146 may include avariety of shapes, shown here as two notches 146, that are in fluidcommunication with the lumen 112. The two circumferentially-spaced(illustrated as diametrically opposed) notches 146 extend longitudinallyand proximally from the distal tip end 142 and between the lumen 112 andthe outer surface 138 of the tip 110, radially. While the particularillustrative embodiment of FIGS. 2 and 3 includes two notches 146, itwould be understood that any numbers of openings 146, or apertures, ofvarious shapes or sizes may be used. The size and number of the notches146 may be selected so that the summed total cross-sectional area of allnotches 146 is about the same as, or greater than, the smallestcross-sectional area of the lumen 112. This configuration avoids areduction in the flow of blood in the event that the distal tip end 142becomes obstructed or occluded during pump operation. Whether or notsuch blockage occurs is a function of the proximity of the distal tipend 142 to the inside surface of the biologic tissue through which thetip 110 extends and the minimum hydrostatic pressure within the chamberas blood is pumped into the inflow cannula 50. More particularly, a dropin the chamber's hydrostatic pressure during pump operation may causethe chamber to sufficiently collapse such that the biologic tissuecontacts the tip 110 and at least partially obstructs the distal tip end142. If such a block should occur with a tip constructed in accordancewith an embodiment with the present invention, then continued operationof the pump 28 may proceed by the influx of blood to the lumen 112 viathe notches 146. Therefore, an undesirable interruption in the flow ofblood into the inflow cannula 50 may be avoided.

An outer surface 150 of the proximal end portion 114 may be polished,sintered, or coated with a material that promotes, or accelerates, woundhealing of the biologic tissue in contact with the outer surface 150when the tip 110 is inserted into the biologic tissue. Suitablematerials may include, but are not limited to, calcium phosphate andcollagen. The portions of the outer surface 138 of the tip 110 that areexposed to blood may include an anti-thrombotic coating to minimizethrombus formation. Examples of anti-thrombotic coating materials thatmay be used include, but are not limited to, heparin, and silver.

Referring now to FIGS. 2-4, the shaft 120 may be secured to the tip 110and the hub 130 by thermal bonding, a molding process, or by othermeans, such as the application of sufficient temperature and pressure tothe parts to be bonded. The shaft 120 may be constructed as a unitarystructure with the tip 110, and the hub 130 thermally bonded thereto.Alternatively, the shaft 120 may have a composite construction, anexample of which is shown in the cross-sectional view in FIG. 4. In theillustrative embodiment, the shaft 120 may include an inner liner 152, areinforcing structure 154 that is secured to the inner liner 152, and anouter jacket 156 that is secured to both the reinforcing structure 154and the inner liner 152. Accordingly, and as shown in FIG. 4A, the innerliner 152 may be tubular and defines the lumen 122 of the shaft 120. Theinner liner 152 may be a co-extruded liner having inner and outerportions 158, 160, which combine to define a wall thickness (designatedas t_(sum)) of the inner liner 152. The inside diameter of the innerportion 158, which corresponds to the diameter of the lumen 122, mayvary depending upon the desired blood flow rate for the particularapplication. Generally, the lumen 122 will have the same diameter as thelumen 132 of the hub 130 and the lumen 112 of the tip 110. For example,the diameter of the lumen 122 may vary from about 0.040 inch (1.016 mm)to about 0.400 inch (10.016 mm). The overall wall thickness of the shaft120 may vary depending upon the desired mechanical performancecharacteristics (bending, column strength, torsional strength, etc.) ofthe shaft 120. For example, the wall thickness of the shaft 120 may varyfrom about 0.004 inch (0.1016 mm) to about 0.080 inch (2.032 mm).

The inner portion 158 of the inner liner 152 may be constructed from athermoset material or a thermoplastic material having a relatively highdurometer, for example, ranging from about shore 55 D to about shore 80D and with a thickness, t₁, that may range from about 0.0005 inch(0.0127 mm) to about 0.0050 inch (1.27 mm). Suitable thermoset materialsmay include, but are not limited to, an etched fluropolymer andpolyimide. Examples of suitable thermoplastic materials include, but arenot limited to polyamide, polyurethane, and polyethylene. An example ofa polyurethane that may be used is CARBOTHANE.

The outer portion 160 of the inner liner 152 may be constructed from athermoplastic material having a lower durometer, for example, rangingfrom about shore 25 A to shore 60 A, and a thickness, t₂, that may rangefrom about 0.0005 inch (0.0127 mm) to about 0.0100 inch (0.254 mm). Anexample of a suitable material that may be used is a polyurethane, suchas CARBOTHANE.

The reinforcing structure 154 may be overlayed onto the outer portion160 of the inner liner 152 and may have a braided construction as shownin FIG. 3 or a coiled construction as shown in FIG. 2. The reinforcingstructure 154 may be constructed from a metal wire, such as stainlesssteel or titanium wire, but may also be made from a polymeric material,such as KEVLAR (E.I. du Pont de Nemours and Co., Wilmington, Del.).Further, the construction material may have various cross-sectionalshapes, including, but not limited to, round and rectangular. If a roundwire is used, the wire diameter may typically vary from about 0.001 inch(0.0254 mm) to about 0.005 inch (0.127 mm). If the material used has arectangular cross-section, the rectangle may typically have a heightranging from about 0.001 inch (0.0254 mm) to about 0.005 inch (0.127 mm)and a width ranging from about 0.003 inch (0.0762 mm) to about 0.010inch (0.254 mm).

The coiled construction of FIG. 2 may include a coil pitch ranging fromabout 0.001 inch (0.0254 mm) to about 0.060 inch (1.524 mm), dependingon the particular wire used and the diameter of the lumen 122. In someembodiments, the coil pitch may vary along the length of the shaft 120with the higher coil pitch being located distally to increaseflexibility distally. With a braided construction, shown in FIG. 3, thebraid pic rate (i.e., the number of cross-overs per inch of braid) mayrange from about 10 ppi to about 100 ppi; in some embodiments, the picrate may vary along the length of the shaft 120 with higher pic ratespositioned distally, again for increased flexibility.

The outer jacket 156 is applied over the inner liner 152 and thereinforcing structure 154 to complete the composite construction. Theouter jacket 156 may be constructed from a thermoplastic material, suchas a polyurethane, having a durometer ranging from about shore 25 A toabout shore 60 A. The material of the outer jacket 156 is selected to becompatible with the materials of the outer portion 160 of the innerliner 152 and of the reinforcing structure 154. This attention tocompatibility ensures complete encapsulation of the reinforcingstructure 154 and complete polymeric bonding between the outer jacket156 and the inner liner 152, which prevents de-lamination.

In some embodiments, the inner and outer portions 158, 160 may beconstructed from similar, or the same, material; however, this is notrequired.

Though not specifically shown, the shaft 120 may include barbs and/or acannula stop that aid in the assembly of the tip 110 to the shaft 120.The barbs provide an interference fit between the shaft 120 and the tip110, while the stop ensures complete insertion of the shaft 120 into thetip 110.

Referring still to FIG. 2 where one exemplary embodiment of the hub 130is shown and includes an inner cylindrical portion 162 that extends fromthe proximal end portion 134 to the distal end portion 136. The hub 130may further include a plurality of longitudinally-spaced, annularmembers 164 that are integral with, and extend around, the cylindricalportion 162. The annular members 164 control a kink radius of the hub130 and allow a physician to trim the length of the hub 130 to conformto the particular anatomy of the patient 22. The kink radius may beconsidered to be the bend radius of the shaft 120 that would result in alocal deformation, or kinking, of the shaft 120. In FIG. 2, the annularmembers 164 are spaced equally by a predetermined distance, d₁. Thephysician may trim the hub 130 to the required length by cutting thecylindrical portion 162 between adjacent ones of the annular members 164to provide the desired length of the hub 130. The distal end portion 136of the hub 130 may be devoid of the annular members 164 in order tofacilitate bonding of the distal end portion 136 of the hub 130 to theproximal end portion 124 of the shaft 120.

FIG. 5 illustrates an alternative embodiment of a hub 130′ that includesa distal-most annular member 164 a that is longitudinally-spaced fromthe adjacent annular member 164 b by a distance, d₂, that is greaterthan d₁, defined above. The size of d₂ may be selected to accommodate aflow sensor 166, shown in phantom, which may be used to measure theblood flow rate through the inflow cannula 50. The flow sensor 166 maybe any commercially available product, such as the flow meters that arecommercially available from Transonic Systems, Inc. (Ithaca, N.Y.), thatcircumvent the hub 130, and that operate by an ultrasonic technology.The flow sensor 166 may be clipped, or otherwise secured, to the hub130. Wires or cables associated with the flow sensor 166 may be routedwith the power cord 34 (FIG. 1A) associated with the pump 28 (FIG. 1).

The construction material of the hub 130 may be selected from knownmaterials, for example, a thermoset material such as silicone, or athermoplastic material, such as polyurethane. The selected material mayhave a durometer that varies from about shore 25 A to about shore 75 Aand may have a stiffness generally equivalent to, or greater than, theoverall stiffness of the composite structure of the shaft 120. The hub130 may then be molded or bonded to the proximal end portion 124 of theshaft 120.

One illustrative procedure for connecting the inflow cannula 50 to theheart 20 is shown in FIGS. 6A-6D with additional reference made to FIG.1A. While the method includes the tip 110 from FIG. 2, it would beunderstood that any design, including those illustrated herein, may beincorporated.

In FIG. 6A, the physician punctures the wall 52 with a guide-wire 168 ata surgical site 169. A dilator device 170, which includes a tip 172 thatis secured to a shaft 174 having a lumen 175 configured to accept theguide-wire 168, is backloaded over the guide-wire 168 and delivered tothe wall 52 of the heart 20. The inflow cannula 50 is backloaded overthe dilator device 170 and advanced to the wall 52 of the heart 20.

As FIG. 6A illustrates, a distal portion of the guide-wire 168 may belooped, coiled, or j-shaped, at least partially, to help avoid trauma tothe tissue of the heart 20 during and after insertion.

The tip 172 of the dilator device 170 generally includes a conical shapethat may be used to gradually dilate a puncture in the wall 52 that wascreated by the guide-wire 168. This gradual dilation facilitates theinsertion of the tip 110 through the wall 52. Insertion is furtherfacilitated by the frusto-conical shape of the distal end portion 116 ofthe tip 110.

FIG. 6B illustrates a subsequent step with the entire distal end portion116 of the tip 110 inserted into the left ventricle 26. After insertion,the inflow cannula 50 may be retracted slightly so that the shoulder 140of the tip 110 is positioned against the inside surface of the wall 52,acting as a firm stop and providing a perceptible feedback to thephysician.

With the tip 110 so positioned, purse string sutures 176, 178 may beused to tie off and fully secure the inflow cannula 50 to the wall 52,as shown in FIG. 6C. If necessary, additional tissue may be gatheredwith additional purse string sutures (not shown), though this is notspecifically shown. As discussed previously, the outer surface 150 ofthe proximal end portion 114 of the tip 110, which extends across thepuncture in the wall 52, may be coated with a material that promotes, oraccelerates, wound healing of the vascular tissue that is in contactwith the outer surface 150. This may further aide in providing a leaktight seal.

FIG. 6D illustrates the surgical site 169 after the sutures 176, 178have been tightened and the dilator device 170 with the guide-wire 168are retracted from the left ventricle 26. As a result, the distal endportion 116 of the tip 110 remains inserted in the left ventricle 26 andis secured to the wall 52 of the heart 20.

It will be readily appreciated that the procedure illustrated in FIGS.6A-6D is a just one exemplary surgical based procedure for inserting thetip 110. Alternatively, the procedure could include a lateralthoracotomy to access the left atrium 24 so that the tip 110 is anchoredat a location on the postero-medial wall, near an intra-atrial septum180, at the so called “Waterson's Groove”; a thoracoscopic surgery wherea tubular trocar is used to access the intra-thoracic location(Waterson's Groove, for example); or an over-the-wire (Seldinger)technique where a needle crosses the intra-atrial septum 180, aguide-wire may be placed therethrough, and a specialized introductionobtuator (or a dilator device) may be used in advancing the inflowcannula 50 into the intra-atrial septum 180, as described in greaterdetail below.

One of ordinary skill would readily appreciate that the openingextending proximally relative to the distal tip end may be constructedto include any number of alternate configurations beyond the embodimentshown in FIGS. 2-3. For example, FIG. 7 illustrates a tip 182 that, likethe tip 110 of FIGS. 2-3, includes at least one opening 183 configuredto permit a continuous flow of blood even in the event of partial orcomplete blockage or occlusion. In that regard, the tip 182 includesproximal and distal end portions 184, 186 with a lumen 188 extendingtherebetween and may be constructed and manufactured similarly to thetip 110 of FIG. 3. The proximal and distal end portions 184, 186 may beseparated by an annular member, or seating ring 190, that is configuredto operate in a manner that is similar to the shoulder 140 of the tip110 shown in FIG. 3, i.e., as a positive stop during insertion. Theproximal end portion 184 is secured to the distal end portion 126 of theshaft 120, as described previously, and such that the lumen 188 of thetip 182 is in fluid communication with the lumen 122 of the shaft 120.

The at least one opening 183 is defined by a plurality of notches, i.e.,openings 183 extending proximally from the distal tip end 193, andindeed being coextensive with the distal end tip 193. Accordingly, thedistal tip end 193 may be constructed to be substantially perpendicularto a lengthwise central axis 194. In the illustrative embodiment, thenotches 183 are equally spaced circumferentially; however, this spacingarrangement is not required. Further, while four notches 183 are shown,it would be understood that the number of notches 183 may vary from two(shown in FIG. 3) to eight and would depend on the cross-sectional areaof the lumen 188, the lengths of the notches 183, and/or the widths ofthe notches 183. Stated another way, the number and configuration of thenotches 183 may be selected such that the total cross-sectional flowarea of all notches 183 is approximately the same as the cross-sectionalarea of the lumen 188 in order to avoid restriction of blood flow.

FIGS. 8 and 8A illustrate yet another embodiment of a tip 196 thatincludes proximal and distal end portions 198, 200 with a lumen 202extending therebetween. As stated before, the proximal end portion 198is secured to the distal end portion 126 of the shaft 120 such that thelumen 202 of the tip 196 is in fluid communication with the lumen 122 ofthe shaft 120. Further, and similar to the tip 182 of FIG. 7, the tip196 may include a seating ring 204 separating the proximal and distalend portions 198, 200 and is configured to be positioned against theinside surface of a tissue wall 52 (FIG. 1A).

In the illustrative embodiment, the opening 206 in the tip 196 isdefined by an inclined edge that extends proximally from a distal tipend 207 of the tip 196. The degree of inclination may be an angle, α,that varies relative to a longitudinal centerline axis 208 of the tip196 from about 15° to about 75°.

The distal end portion 200 includes a second opening 210 extendingproximally relative to the distal tip end 207, shown herein as anaperture 210 that is enclosed by the material comprising the tip 196 andthat extends between the lumen 202 and an outer surface 212 of the tip196. While only one aperture 210 is shown, it would be understood thatthe distal end portion 200 may alternatively include a plurality ofapertures.

During normal pump operation, the likelihood that the inclined edge 206would become blocked is significantly reduced. In this manner, theproximally extending opening 206 will help to assure blood flow into thelumen 202. However, should the blood flow through the inclined edge 206be reduced, then blood flow may continue through the second opening 209,the aperture 210. In this way, the tip 196 provides two manners ofpreventing blood flow reduction.

In still other embodiments, a tip may be constructed in a manner thatreduces the need for purse string sutures. Additionally, and/oroptionally, a tip may be constructed in a manner that facilitates use ina less-invasive, catheter-based surgical procedure, such as thosedescribed in U.S. patent application Ser. No. 12/256,911, published asU.S. Patent Appl. Publ. No. 2009/0112050 and entitled “TransseptalCannula, Tip, Delivery System, and Method,” the disclosure of which isincorporated herein by reference in its entirety.

One exemplary embodiment of a suitable tip design is shown in FIG. 9 andincludes a tip 250 having a truncated frusto-conical shape that issimilar to the shape described previously with reference to FIG. 3. Thetip 250 has a proximal end 252 and a distal end 254 with a lumen 256extending therebetween that is collinear with the lumen 122 (FIG. 2) ofthe shaft 120. The distal end 254 includes at least one opening 258,defined in FIG. 9 as two notches, that extend proximally from a distaltip end 260.

Referring still to FIG. 9 and also now to FIG. 9A, the tip 250 furtherincludes a first anchor 262 having a plurality of struts 264 asdescribed in U.S. patent application Ser. No. 12/720,012, published asU.S. Patent Appl. Publ. No. 2010/0249490 and entitled “TransseptalCannula Device, Coaxial Balloon Delivery Device, and Methods of Usingthe Same,” the disclosure of which is incorporated herein by referencein its entirety. It should be appreciated that while four struts 264 areshown, this number is not so limited but rather an anchor could beenvisioned where fewer or more struts may be necessitated or desired fora particular physician's needs or preference. Yet, providing at leastthree struts 264 may result in greater stability of the implanted tip250.

The struts 264 of the first anchor 262 may be at least partiallyconstructed from a superelastic NiTi material by chemically etching theparts from flat sheet stock, electropolishing the etched parts to removerough edges generated during the formation process, and then heating theparts to a superelastic state. However, other suitable biocompatible,non-compliant, flexible material would be sufficient. As is shown, thestruts 264 extend from a common ring structure 266 that is affixed intoa groove 268 within the tip 250 with glue, epoxy, friction fit, or otherknown means. As a result, the struts 264 of the first anchor 262 mayextend radially, in a deployed position, from the common ring structure266 and relative to the lengthwise central axis 269. In this deployedposition, the first anchor 262 is configured to be positioned along afirst side of the biologic tissue, shown here as the intra-atrial septum180 between the right and left atria 54, 24. The superelastic state ofthe struts 264 allows the struts 264 to be deflected to a collapsedposition (shown in phantom) that is directed angularly away from thedeployed position (shown in solid). This collapsible nature of the firstanchor 262 enables the tip 250 to be preloaded into a delivery sheath(not shown) and reduces the invasiveness of the procedure. Morespecifically, the struts 264 of the first anchor 262 are deflected in adistal direction and the inflow cannula 50 back-loaded into the deliverysheath. The distally directed struts 264 are thus positioned fordeployment, as shown in phantom in FIG. 9A. If desired, a ballooncatheter may be directed through the lumen of the shaft 120 and the tip250. The balloon, when inflated contacts the inner diameter of the tip250. This contact between the tip 250 and the balloon allows thephysician to manipulate the position of the tip 250 within the deliverysheath. After the tip 250 is positioned within the intra-atrial septum180 and the first anchor 262 deployed, the delivery sheath may beretracted from the surgical site. Alternatively, the delivery sheath maybe constructed from a peel away material such that the delivery sheathis split and removed from the surgical site.

Referring still to FIGS. 9 and 9A, the proximal end portion 252 of thetip 250 may be shaped to receive and secure a second anchor 270 thatincludes a plurality of struts 272 coupled to a band 274. The struts 272may be constructed to extend from a common ring structure 276 that isaffixed within a groove 278 of the band 274. The struts 272 of thesecond anchor 270 may be operable to move from a contracted state (forinsertion as described below) to an extended state and may be machinedfrom a tubular structure formed using wire or formed from a flat sheetstock, as was described above. The wire or flat sheet stock may be anyshape-memory material (such as nickel titanium, NiTi, or MP35N). Whilemany shapes for the struts 272 are possible, the shape shown includes anangled portion 272 a and a contact portion 272 b when the strut 272 isin the extended state. The contact portion 272 b will contact thebiologic tissue while the angled portion 272 a allows the anchor 270 toaccommodate a wide range of anatomies and tissue thicknesses. The angledportion 272 a also creates a force that will resist a distal movement ofthe anchor 170 after it has been properly attached to the tip 250.

The band 274 may be constructed from materials and using methods thatare similar to the tip 250. As shown in FIG. 9A, the band 274 is shapedand sized to be received by the proximal end portion 252 of the tip 250,and secured by friction fit, interference fit, a magnet, a screw threador other in vivo assembly methods that are generally known.

For delivery, the second anchor 270 is positioned onto a first deliverysheath 242 having notches 244 in which the plurality of struts 272 restin a contracted state and in a proximal direction. The notches 244contribute to the over-all low profile assembly for percutaneousdelivery of the second anchor 270. The first delivery sheath 242 and thesecond anchor 270 are preloaded into a second delivery sheath 248 and,as a unit, are percutaneously directed to the previously inserted tip250. With sufficient distally-directed force, the band 274 is attachedto the proximal end portion 252 of the inserted tip 250 by a mechanicalconnection. The plurality of struts 272 are then deployed by retractingthe second delivery sheath 248 from the intra-atrial septum 180, whichmay include pulling on one or more connector members 246 that extendproximally from the second delivery sheath 248 into the hub catheterinsertion site (not shown). After sufficient retraction, the struts 272deploy from the contracted state to the deployed state against theintra-atrial septum 180. Both of the first and second delivery sheaths242, 248 may then be retracted away from the tip 250.

As is further shown in FIG. 9, the struts 264, 272 of one or bothanchors 262, 270 may include a porous polymeric structure 280 to providea larger surface for engaging the intra-atrial septum 180 (FIG. 9A) thanthe plurality of struts 264, 272 alone. The porous polymeric structure280 may also allow for tissue in-growth, wherein biologic tissue fromthe intra-atrial septum 180 may grow and embed within the porouspolymeric structure 280 to provide greater structural stability andsealing capacity. Suitable materials for the porous polymeric structure280 may include, but are not limited to, polyester monofilament ormultifilament yarn; ePTFE monofilament or multifilament yarn; orfluorinated polyolefin fibers or yarns, which can be woven, braided,knitted, or felted into a proper configuration. The porous polymericstructure 280 may further include various intrinsic configurationsincluding weaves, braids, or knits having two or three-dimensionalhoneycombs, circular, flat, or tri-axial tubular structures. In otherembodiments, the porous polymeric structure 280 may be constructed froman ePTFE piece in tubular, cylindrical, or sheet form. Generally, theporous polymeric structure 280 will be constructed by etching or lasercutting a shape from two sheets of a stock material (such as thosedescribed above). The shaped polymeric structures 280 are thenultrasonically welded together such that the shaped polymeric structures280 capture the struts 264, 272 therebetween.

FIG. 9 further illustrates that the anchors 262, 270 may be positionedsuch that the struts 264 of the first anchor 262 are offset with respectto the struts 272 of the second anchor 270. This configuration hasparticular load-bearing benefits but should not be considered to berequired.

Turning now to FIGS. 10 and 10A were yet another illustrative embodimentof a tip 286 is shown. The tip 286 is constructed in a manner that issimilar to the tip 182 (FIG. 4) but includes a first anchor 288 and anengagable second anchor 290 that are similar to those shown in FIG. 9but without including the porous polymeric structure 280 (FIG. 9). Theanchors 288, 290 each include a plurality of struts 292 for residing onopposing sides of the intra-atrial septum 180. The tip 286 furtherincludes at least one opening 294, illustrated as a plurality ofnotches, extending proximally from a distal end 298 for providingfluidic access to the lumen 296 of the tip 286 should the distal tip end298 become occluded or obstructed.

FIGS. 11 and 11A illustrate yet another embodiment of a one-pieceintra-septal tip 300 having first and second anchors 302, 304 coupledthereto and each including a plurality of struts 305 that may bepercutaneously delivered to the biologic tissue with a single deliverysheath 318. The tip 300 includes one or more rings 306 that are providedfor several reasons. These rings 306 may act in a manner so as to engagethe anchors 302, 304 and/or act in cooperation with one or more clamps308 to affix the anchors 302, 304 on the tip 300. Suitable clamps 308may include swage or crimp-style clamps or may be attached to the tip300 by an adhesive, welding, or tying.

The tip 300, as shown, further includes a structure that is similar tothe tip 196 of FIG. 5 having two openings 310, 312, e.g., the opening310 defined by an inclined distal end surface that extends proximallyfrom a distal tip end 313 of the tip 196 and the opening 312 defined byan opening in the form of an aperture. The openings 310, 312 reduce thelikelihood of blockage or flow restriction into the lumen 314 wheninserted through the intra-atrial septum 180. The tip 300 furtherincludes barbs 316 for providing a frictional fit with the shaft 120.

While the present invention has been illustrated by a description ofvarious illustrative embodiments and while these embodiments have beendescribed in some detail, it is not the intention of the Applicants torestrict or in any way limit the scope of the appended claims to suchdetail. Additional advantages and modifications will readily appear tothose skilled in the art. The various features of the invention may beused alone or in any combinations depending on the needs and preferencesof the user. However, the invention itself should only be defined by theappended claims.

What is claimed is:
 1. A cannula for insertion through a biologictissue, the cannula comprising: a shaft comprising proximal and distalend portions and a lumen extending therebetween; a tip having a proximalend portion, a distal tip end, and a lumen extending therebetween, theproximal end portion of the tip being secured to the distal tip end ofthe shaft, and a hub having proximal and distal end portions and a lumenextending therebetween, the distal end portion of the hub positioned atthe proximal end portion of the shaft such that the lumen of the hub isin fluid communication with the lumen of the shaft, and the proximal endportion of the hub is configured to be coupled to an auxiliary device,the tip having a first distal tip opening at the distal tip end and asecond opening communicating with the lumen of the tip, the secondopening extending proximally relative to the distal tip end, wherein thesecond opening of the tip extending proximally is configured to permitfluid to be continuously drawn into the lumen of the tip even in theevent the distal tip opening becomes obstructed.
 2. The cannula of claim1, wherein the hub further comprises an inner cylindrical portion and aplurality of outer, longitudinally spaced annular members that areformed integral with the inner cylindrical portion, the longitudinallyspaced annular members operable to control a kink radius of the hub. 3.The cannula of claim 1, wherein the shaft further comprises a compositeconstruction comprising an inner liner, a reinforcing structure securedto the inner liner, and an outer jacket secured to the reinforcingstructure and the inner liner.
 4. The cannula of claim 3, wherein theinner liner comprises a co-extruded inner layer defining the lumen ofthe shaft and an outer layer bonded to the co-extruded inner layer. 5.The cannula of claim 4, wherein the co-extruded inner layer of the innerliner is made from a first thermoplastic material and the outer layer ofthe inner liner is made from a second thermoplastic material differentfrom the first thermoplastic material.
 6. The cannula of claim 3,wherein the outer jacket is bonded to the reinforcing structure and theinner liner.
 7. The cannula of claim 3, wherein the reinforcingstructure comprises a braided construction.
 8. The cannula of claim 3,wherein the reinforcing structure is made from a metallic material or apolymeric material.
 9. The cannula of claim 3, wherein the reinforcingstructure comprises a coiled configuration.
 10. The cannula of claim 1,wherein the second opening extending proximally includes at least oneaperture extending between the lumen and an outer surface of the tip.11. The cannula of claim 1, wherein the second opening extendingproximally includes at least one notch extending proximally from thedistal tip end and between the lumen and an outer surface of the tip.12. The cannula of claim 1, wherein the second opening extendingproximally includes a plurality of notches extending proximally from thedistal tip end and between the lumen and an outer surface of the tip,the plurality of notches being spaced circumferentially around the tip.13. The cannula of claim 1, wherein the second opening extendingproximally includes an inclined edge extending proximally from thedistal tip end, wherein the inclined edge is angled relative to alengthwise central axis of the tip.
 14. The cannula of claim 13, whereinthe tip further includes a third opening extending proximally relativeto the distal tip end, the third opening including at least one notch orat least one aperture.
 15. The cannula of claim 1, wherein the tipfurther includes an outer surface having a frusto-conical shape thatconverges distally.
 16. The cannula of claim 15, wherein the outersurface includes a shoulder configured to abut a first side of thebiologic tissue when the tip is positioned through the biologic tissue.17. The cannula of claim 16, wherein the shoulder is further configuredto center the tip relative to the insertion position and to preventtissue obstruction.
 18. The cannula of claim 1, wherein the tip isconstructed from a material that is molded such that the lumen is devoidof parting lines.
 19. The cannula of claim 1, the tip is constructedfrom a metallic material.
 20. The cannula of claim 19, wherein at leasta portion of an outer surface of the tip promotes tissue in-growth. 21.The cannula of claim 1, wherein the tip further includes a first anchorthat is configured to be deployed from a contracted state to an expandedstate, wherein the first anchor is configured to engage at least oneside of the biologic tissue in the expanded state and is operable toresist movement of the tip in at least one direction along a lengthwisecentral axis of the tip.
 22. The cannula of claim 21, wherein the firstanchor further comprises a plurality of struts extending generallytransverse to the lengthwise central axis of the tip.
 23. The cannula ofclaim 22, wherein the plurality of struts is formed from a superelasticmaterial and are folded to a position generally parallel with thelengthwise central axis when in the contracted state and extend to aposition generally transverse to the lengthwise central axis when in theexpanded state.
 24. The cannula of claim 22, wherein the first anchorfurther includes a porous polymeric structure coupled with the pluralityof struts to facilitate tissue in-growth for securing the first anchorto the biologic tissue.
 25. The cannula of claim 21 further comprising:a second anchor located proximal to the first anchor, the second anchoroperable to prevent a movement of the tip in a distal direction.
 26. Thecannula of claim 25, wherein the second anchor further comprises aplurality of struts extending generally transverse to the lengthwisecentral axis of the tip.
 27. The cannula of claim 26, wherein theplurality of struts is formed from a superelastic material and arefolded to a position generally parallel with the lengthwise central axiswhen in the contracted state and extend to a position generallytransverse to the lengthwise central axis when in the expanded state.28. The cannula of claim 26, wherein the second anchor further includesa porous polymeric structure coupled with the plurality of struts andfacilitating tissue in-growth for securing the second anchor to thebiologic tissue.
 29. A cannula for insertion through a biologic tissue,the cannula comprising: a shaft comprising proximal and distal endportions and a lumen extending therebetween; and a tip having a proximalend portion, a distal tip end, and a lumen extending therebetween, theproximal end portion of the tip being secured to the distal tip end ofthe shaft, the tip having a first distal tip opening and a secondopening communicating with the lumen of the tip, the second openingextending proximally relative to the distal tip end, wherein the secondopening of the tip extending proximally is configured to permit fluid tobe continuously drawn into the lumen of the tip even in the event thedistal tip opening becomes obstructed, wherein the tip is constructedfrom a thermoplastic material or a thermoset material and an innersurface of the tip includes an anti-thrombotic coating.
 30. The cannulaof claim 29, wherein an outer surface of the tip further includes apolymeric coating.
 31. The cannula of claim 29, wherein an outer surfaceof the proximal end portion of the tip includes a coating that promotesthrombus formation.
 32. A delivery system comprising: a shaft comprisingproximal and distal end portions and a lumen extending therebetween; anda tip having a proximal end portion, a distal tip end, and a lumenextending therebetween, the proximal end portion of the tip beingsecured to the distal tip end of the shaft, the tip having a firstdistal tip opening at the distal tip end and a second openingcommunicating with the lumen of the tip, the second opening extendingproximally relative to the distal tip end, wherein the second opening ofthe tip extending proximally is configured to permit fluid to becontinuously drawn into the lumen of the tip even in the event thedistal tip opening becomes obstructed, wherein the tip further includesa first anchor that is configured to be deployed from a contracted stateto an expanded state, wherein the first anchor is configured to engageat least one side of the biologic tissue in the expanded state and isoperable to resist movement of the tip in at least one direction along alengthwise central axis of the tip, and a delivery sheath configured toreceive the cannula and to move relative thereto for deploying the firstanchor into the expanded state.
 33. The delivery system of claim 32,wherein the delivery sheath is constructed from a peel-away material.